ARM (Advancement of Research for Myopathies) is a 501(c)(3) non-profit organization with the primary goal of speeding up bio-medical research on IBM2, the Autosomal Recessive form of Hereditary Inclusion Body Myopathies (HIBM).
Founded by HIBM patients in 2000, ARM's mission is to support and inform patients and their families, to raise funds for research, to encourage researchers to study this rare disorder and to ultimately find a cure for Hereditary Inclusion Body Myopathy (HIBM). ARM, a non-profit organization, is the leading source of information, hope and knowledge for HIBM patients worldwide, and is the only non-profit organization specialized in this rare disorder. ARM offers scientific grants to research centers who are interested in working towards developing a treatment for HIBM.
Every year unsuspecting young adults are diagnosed with Hereditary Inclusion Body Myopathy (HIBM), a rare muscle wasting disorder for which there is no treatment or cure yet available. For them and all HIBM patients, ARM offers a ray of hope with research funding, support and an expanding campaign of public awareness. Only with your help can ARM continue its efforts to cure this debilitating disease.
Read the story about two brothers, Dr. Daniel and Dr. Babak Darvish, whom in their 20's (1997) started experiencing HIBM symptoms during medical school. Living with such a powerful disease inspired them to come forward and dedicate their lives to research and finding a cure and thus formed ARM, a non-profit organization.
Read the History of ARM and how it all began.